| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145082.2 | 597 | Missense Mutation | TCG,TTG | S97L | NP_001138554.1 |
| NM_001145083.1 | 597 | Intron | NP_001138555.1 | ||
| NM_001145093.2 | 597 | Intron | NP_001138565.1 | ||
| XM_006713112.2 | 597 | Intron | XP_006713175.1 | ||
| XM_006713113.3 | 597 | Intron | XP_006713176.1 | ||
| XM_011533607.1 | 597 | Missense Mutation | TCG,TTG | S97L | XP_011531909.1 |
| XM_011533608.1 | 597 | Intron | XP_011531910.1 | ||
| XM_017006225.1 | 597 | Intron | XP_016861714.1 |